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Translational research: Find the needle in the haystack and access trustworthy knowledge of known variants
As WES NGS experiments become broader and more sophisticated, variant assessment and staying up-to-date with published disease-causing variants becomes increasingly difficult and time-consuming.

Join this 1-hour webinar and we will show how to identify disease-relevant genes and variants and how use contextually relevant information to annotate and prioritize causal variants.

Learn how to:
- Filter/prioritize variants to identify causal variants underlying inherited diseases and traits
- Access trustworthy information of known variants in disease-relevant genes for panel development or assay design

Get connected to the industry’s most comprehensive collection of biological and clinical findings to advance your translational research. Whether you are searching for a “variant needle” in a “data haystack” or need access to trustworthy information about known variants, we have a solution with the depth and breadth you need.

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Nov 25, 2020 10:00 AM in Copenhagen

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Webinar is over, you cannot register now. If you have any questions, please contact Webinar host: Simon Nielsen.